BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SKLAR INSTRUMENTS

    MDR report key: 22113732 · Received May 30, 2025

    Report

    Report Number
    22113732
    Event Type
    Malfunction
    Date Received
    May 30, 2025
    Date of Event
    April 28, 2025
    Report Date
    May 21, 2025
    Manufacturer
    SKLAR CORPORATION
    Product Code
    LRW
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    UT
    Reporter Occupation
    003

    Narratives

    Description of Event or Problem · 0

    BURR ON TIP OF SCISSORS, CAUSED A SUPERFICIAL SKIN TEAR ON PATIENT'S LEG. MANUFACTURER RESPONSE FOR SCISSORS, GENERAL, SURGICAL, SKLAR INSTRUMENTS (PER SITE REPORTER). WAITING FOR THEIR RESPONSE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    579229 SKLAR INSTRUMENTS SCISSORS, GENERAL, SURGICAL LRW SKLAR CORPORATION 96-2502 (10)600026

    Patients

    Seq Age Sex Outcome Treatment
    1 83 YR Female